Herbert Jägle

Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel

Susanne Kohl, Tim Marx, Ian Giddings et al. · Nature Genetics · 1998 · 339 citations

Medicine, Genetics, Molecular Genetics +13

CNGA3 Mutations in Hereditary Cone Photoreceptor Disorders

Bernd Wissinger, Daphne Gamer, Herbert Jägle et al. · The American Journal of Human Genetics · 2001 · 326 citations · Full text

Medicine, Genetics, Molecular Genetics +14

CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

Susanne Kohl, Balázs Varsányi, Gesine Abadin Antunes et al. · European Journal of Human Genetics · 2004 · 251 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

A luminous efficiency function,<i>V</i>*(<i>λ</i>), for daylight adaptation

Lindsay T. Sharpe, Andrew Stockman, Wolfgang Jagla et al. · Journal of Vision · 2005 · 223 citations · Full text

Medicine, Optometry, Vision Science +13

Reorganization of human cortical maps caused by inherited photoreceptor abnormalities

Heidi A. Baseler, Alyssa A. Brewer, Lindsay T. Sharpe et al. · Nature Neuroscience · 2002 · 178 citations

Medicine, Genetics, Neuroscience +14